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The results from this work highlight the importance of considering strain-rate dependences (model II) to provide reliable predictions under dynamic loading scenarios. In this regard, rate-independent approaches (model I) are rather limited to quasi-static loading.The early and late development of new anticancer drugs, small molecules or peptides can be slowed down by some issues such as poor selectivity for the target or poor ADME properties. Computer-aided drug design (CADD) and target drug delivery (TDD) techniques, although apparently far from each other